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wht didt u get?Again plz
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wht didt u get?Again plz
wht didt u get?
thanks alotwhen both double bonds break bw carbons two ketones r formed nd 1 is already present so its 3
after 2005 but i dont really remember sorrythanks alot
can you tell me in your paper
question repeated from recent papers or old papers.
after 2005 but i dont really remember sorry
its not nucleophilic substitution its isomerismcan you please help me with my question
http://papers.xtremepapers.com/CIE/...d AS Level/Chemistry (9701)/9701_s07_qp_1.pdf
Q20 how it is nucleophilic substitution
its not nucleophilic substitution its isomerism
chek againBUT MS ANSWER IS D
yes one flourine substitue chlorineBUT MS ANSWER IS D
In details plzQ7 PH3 has 104
Q12 is B cuz it is least high thn any other option
Q 7 angle 104 cuz it has 3 bonds nd one lone pairIn details plz
Q12 actually i cant under stand it :sQ 7 angle 104 cuz it has 3 bonds nd one lone pair
nd q 12 u understood?
http://papers.xtremepapers.com/CIE/Cambridge International A and AS Level/Chemistry (9701)/9701_w07_qp_1.pdf
Q9 , Q26 . Q37
http://papers.xtremepapers.com/CIE/Cambridge International A and AS Level/Chemistry (9701)/9701_s12_qp_11.pdf
Q21 , 23 , 32
http://papers.xtremepapers.com/CIE/Cambridge International A and AS Level/Chemistry (9701)/9701_s12_qp_12.pdf
Q20 , Q25
http://papers.xtremepapers.com/CIE/Cambridge International A and AS Level/Chemistry (9701)/9701_s07_qp_1.pdf
Q25,26,38
PLZ GUYS
Thnx alotQ20)
When esters are hydrolysed using alkalis under reflux, not only is the reaction a one-way reaction (no equilibrium mixture is formed, reaction is complete) but in the end, the ester is split into an alcohol and acid, the ones that formed it in the first place. However, there is a twist here - the acid reacts with any excess alkali and forms the metal salt of that alkali.
So, in this case we use sodium hydroxide, NaOH, to hydrolyse propyl ethanoate. The products of that hydrolysis are normally Ethanoic Acid, CH3COOH and Propanol, CH3CH2CH2OH. So, the acid forms the Sodium Salt, which means that we get Sodium Ethanoate instead of Ethanoic acid, so we get CH3COONa.
The mass per mole of Propanol is (Mass of all Carbon atoms in molecule + Mass of all Hydrogen atoms in molecule + Mass of all oxygen atoms in molecule) =
(3 * 12 + 8 * 1 + 1 * 16) = 60 grams per mole.
The mass per mole of Ethanoic Acid is (Mass of all Carbon atoms in molecule + Mass of all Hydrogen atoms in Molecule + Mass of all Oxygen atoms in molecule + Mass of all Sodium atoms in Molecule) = (2 * 12 + 3 * 1 + 2 * 16 + 1 * 23) = 82.
Adding this up, the total mass of the organic products (no other carbon-containing products are formed) is equal to 60 + 82 = 142 grams.
The percentage of CH3CH2CH2OH = 60/142 * 100 = 42.25 % = 42.3 %.
The other one must automatically be 100 - 42.3 = 57.7 %.
This means our answer should be C.
I'm running late right now, hope this helped.
Good Luck for all your exams!
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